Canonical Allele Identifier: CA228635483
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs11214606

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439147C>T , CM000673.2:g.113439147C>T GRCh38
NC_000011.9:g.113309869C>T , CM000673.1:g.113309869C>T GRCh37
NC_000011.8:g.112815079C>T NCBI36
NG_008841.1:g.41133G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-14465G>A MANE Select ENSP00000354859.3:p.=
ENST00000346454.7:c.-31-14465G>A ENSP00000278597.5:p.=
ENST00000362072.7:c.-31-14465G>A ENSP00000354859.3:p.=
ENST00000540600.5:n.35-14465G>A
ENST00000542616.1:c.-31-14465G>A ENSP00000441474.1:p.=
ENST00000543292.1:c.-32+8424G>A ENSP00000438419.1:p.=
NM_000795.3:c.-31-14465G>A NP_000786.1:p.=
NM_016574.3:c.-31-14465G>A NP_057658.2:p.=
XM_017017296.2:c.-31-14465G>A XP_016872785.1:p.=
NM_000795.4:c.-31-14465G>A MANE Select NP_000786.1:p.=
NM_016574.4:c.-31-14465G>A NP_057658.2:p.=